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Titlebook: RT-PCR Protocols; Joe O’Connell Book 20021st edition Humana Press 2002

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Detection of mRNA Expression and Alternative Splicing in a Single Cellroy the cell by freezing and thawing, reverse-transcribe RNA, and PCR-amplify. The second step is composed of PCR amplification with another nested PCR-primer set. Using this nested PCR technique, we could detect the expression of FN. We also succeeded in analyzing alternative splicing of FN mRNA in
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RT-PCR for the Assessment of Genetically Heterogenous Populations of the Hepatitis C Virus its antigenicity, is believed to hinder humoral immune-mediated clearance of the virus. The ISDR encodes an approx 40 amino-acid sequence in the C-terminal half of the nonstructural 5A (NS5A) protein. Protein kinase inhibition and transcriptional activation activities have been ascribed to NS5A, bo
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Immuno-PCRhigh specificity of immunocytochemistry, we have developed a new method known as . immuno-PCR to detect antigens at low levels in intact cells or tissue sections (.). The concept of . immuno-PCR is illustrated in .. Our study demonstrated that . immuno-PCR is more sensitive for the detection of Hepa
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Book 20021st editionations of RT-PCR. These include some useful adaptations and applications that could be relevant to the wider research community who are already familiar with the basic RT-PCR protocol. For example, a variety of different adaptations are described that have been employed to obtain quantitative data f
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Triona Goode,Wen-Zhe Ho,Terry O’Connor,Sandra Busteed,Steven D. Douglas,Fergus Shanahan,Joe O’Connel
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Joe O’Connell,Aileen Houston,Raymond Kelly,Darren O’Brien,Aideen Ryan,Michael W. Bennett,Kenneth Nal
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